Device Classification Name |
Immunoelectrophoretic, Immunoglobulins, (G, A, M)
More FDA Info for this Device |
510(K) Number |
K120169 |
Device Name |
Immunoelectrophoretic, Immunoglobulins, (G, A, M) |
Applicant |
GRIFOLS USA, LLC
482 CHERRY LANE RD.
EAST STROUDSBURG, PA 18301 US
Other 510(k) Applications for this Company
|
Contact |
Gary Lehnus
Other 510(k) Applications for this Contact |
Regulation Number |
866.5510
More FDA Info for this Regulation Number |
Classification Product Code |
CFF
Other 510(k) Applications for this Device
More FDA Info for this Product Code |
Date Received |
01/19/2012 |
Decision Date |
08/24/2012 |
Decision |
SESE - SUBST EQUIV |
Classification Advisory Committee |
IM - Immunology |
Review Advisory Committee |
IM - Immunology |
Statement / Summary / Purged Status |
Summary |
Type |
Traditional |
Reviewed By Third Party |
N |
Expedited Review |
|